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Reinvestigations of the reactions of hexachlorocyclotriphosphazene with difunctional primary amines leading to novel dangler, ansa and bridged derivatives. Spectroscopic studies of the derived products

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1 of the 68 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-21): 10.1002/ardp.201100412 (notice 2013-04-02).

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/aoc.3328openalex-snapshot
Synthesis, characterization and catalytic, cytotoxic and antimicrobial activities of two novel cyclotriphosphazene‐based multisite ligands and their Ru(II) complexes
inferredcites →https://doi.org/10.1002/aoc.590070102openalex-snapshot
Coordination and organometallic chemistry of cyclophosphazenes and polyphosphazenes
inferredcites →https://doi.org/10.1002/ardp.201100412openalex-snapshot
Synthesis, Characterization, and Biological–Pharmacological Evaluation of New Phosphazenes Bearing Dioxybiphenyl and Schiff Base Groups
inferredcites →https://doi.org/10.1002/ardp.201370061openalex-snapshot
Arch. Pharm. Chem. Life Sci. (12/2013)
inferredcites →https://doi.org/10.1002/chem.200802413openalex-snapshot
Cyclotriphosphazene Ring as a Platform for Multiporphyrin Assemblies
inferredcites →https://doi.org/10.1002/pi.2030openalex-snapshot
Hydrophobic and superhydrophobic surfaces from polyphosphazenes
inferredcites →https://doi.org/10.1007/s00775-014-1223-5openalex-snapshot
Phosphorus–nitrogen compounds: part 30. Syntheses and structural investigations, antimicrobial and cytotoxic activities and DNA interactions of vanillinato-substituted NN or NO spirocyclic monoferrocenyl cyclotriphosphazenes
inferredcites →https://doi.org/10.1007/s10895-015-1672-4openalex-snapshot
Novel Coumarin Substituted Water Soluble Cyclophosphazenes as “Turn-Off” Type Fluorescence Chemosensors for Detection of Fe3+ ions in Aqueous Media
inferredcites →https://doi.org/10.1007/s10904-007-9126-3openalex-snapshot
Ionic Conductivity of Cross-linked Polymethacrylate Derivatives/Cyclophosphazenes/Li+ Salt Complexes
inferredcites →https://doi.org/10.1007/s10904-007-9132-5openalex-snapshot
From Rings to Polymers
inferredcites →https://doi.org/10.1007/s10973-015-5001-6openalex-snapshot
Phosphorus–nitrogen compounds
inferredcites →https://doi.org/10.1007/s11095-007-9299-zopenalex-snapshot
Biodegradable Poly(2-Dimethylamino Ethylamino)Phosphazene for In Vivo Gene Delivery to Tumor Cells. Effect of Polymer Molecular Weight
inferredcites →https://doi.org/10.1016/0020-1650(80)80125-5openalex-snapshot
Solvent effects in the reactions of N3P3Cl6 with secondary amines
inferredcites →https://doi.org/10.1016/0020-1650(81)80067-0openalex-snapshot
Spirocyclic phosphazenes derived from the reaction of N3P3Cl6 and N4P4Cl8 with bifunctional reagents
inferredcites →https://doi.org/10.1016/0020-1693(94)04162-oopenalex-snapshot
New dioxytetraethyleneoxy macrocyclic cyclophosphazene derivatives
inferredcites →https://doi.org/10.1016/0022-2852(70)90053-6openalex-snapshot
Proton spectra of symmetrical cyclotriphosphazatrienes
inferredcites →https://doi.org/10.1016/0022-2860(78)87282-2openalex-snapshot
Cyclophosphazenes as novel potential antitumor agents: x-ray crystal structure of the octapyrrolidinocyclotetraphosphazene, N4P4(NC4 H8)8
inferredcites →https://doi.org/10.1016/0022-2860(82)90063-1openalex-snapshot
An answer to the spiro versus ansa dilemma in cyclophosphazenes
inferredcites →https://doi.org/10.1016/0022-2860(83)90030-3openalex-snapshot
An answer to the spiro versus ansa dilemma in cyclophosphazenes
inferredcites →https://doi.org/10.1016/0022-2860(84)87244-0openalex-snapshot
An answer to the spiro versus ANSA dilemma in cyclophosphazenes
inferredcites →https://doi.org/10.1016/0022-2860(86)87067-3openalex-snapshot
Attempts at the production of more selective antitumourals
inferredcites →https://doi.org/10.1016/0022-2860(87)80077-7openalex-snapshot
An answer to the spiro versus ANSA dilemma in cyclophosphazenes
inferredcites →https://doi.org/10.1016/0022-2860(90)85029-iopenalex-snapshot
On the antitumor effectiveness of aziridinocyclophosphazenes: crystal and molecular structure of the non-active 2,2-bis (1-aziridinyl)-4,4,6,6-tetrachlorocyclotriphosphazene, gem-N3P3Az2Cl4
inferredcites →https://doi.org/10.1016/b978-0-12-050560-9.x5001-3openalex-snapshot
Phosphorus-nitrogen Compounds
inferredcites →https://doi.org/10.1016/j.biomaterials.2004.02.016openalex-snapshot
Low temperature formation of hydroxyapatite-poly(alkyl oxybenzoate)phosphazene composites for biomedical applications
inferredcites →https://doi.org/10.1016/j.colsurfa.2014.03.022openalex-snapshot
Synthesis and characterization of drug microspheres containing phosphazene for biomedical applications
inferredcites →https://doi.org/10.1016/j.cossms.2007.06.001openalex-snapshot
Recent developments in polyphosphazene materials science
inferredcites →https://doi.org/10.1016/j.ejmech.2012.03.018openalex-snapshot
Synthesis, cytotoxicity and apoptosis of cyclotriphosphazene compounds as anti-cancer agents
inferredcites →https://doi.org/10.1016/j.ejps.2007.12.003openalex-snapshot
Degradable PEG-folate coated poly(DMAEA-co-BA)phosphazene-based polyplexes exhibit receptor-specific gene expression
inferredcites →https://doi.org/10.1016/j.electacta.2012.11.083openalex-snapshot
Lithium polymer cell assembled by in situ chemical cross-linking of ionic liquid electrolyte with phosphazene-based cross-linking agent
inferredcites →https://doi.org/10.1016/j.matlet.2014.03.137openalex-snapshot
Intrinsically fluorescent hollow spheres based on organic–inorganic hybrid polyphosphazene material: Synthesis and application in drug release
inferredcites →https://doi.org/10.1016/j.molstruc.2015.01.033openalex-snapshot
Synthesis, structural characterization and anti-carcinogenic activity of new cyclotriphosphazenes containing dioxybiphenyl and chalcone groups
inferredcites →https://doi.org/10.1016/j.poly.2005.10.023openalex-snapshot
Structural and stereogenic properties of spiro- and ansa-substituted 1,3-propanedioxy derivatives of a spermine-bridged cyclotriphosphazene
inferredcites →https://doi.org/10.1016/j.poly.2007.07.050openalex-snapshot
Formation of spiro and ansa derivatives in the reaction of 2,2,3,3,4,4-hexafluoropentane-1,5-diol with cyclotriphosphazene: Comparison with 2,2,3,3-tetrafluorobutane-1,4-diol
inferredcites →https://doi.org/10.1016/j.poly.2009.07.042openalex-snapshot
Single-, double- and triple-bridged derivatives of cyclotriphosphazenes with an octafluorohexane-1,6-diol
inferredcites →https://doi.org/10.1016/j.poly.2010.07.017openalex-snapshot
Phosphorus–nitrogen compounds: Part 19. Syntheses, structural and electrochemical investigations, biological activities, and DNA interactions of new spirocyclic monoferrocenylcyclotriphosphazenes
inferredcites →https://doi.org/10.1016/j.poly.2010.10.020openalex-snapshot
Effect of chain length on the formation of intramolecular and intermolecular products: Reaction of diols with cyclotriphosphazene
inferredcites →https://doi.org/10.1016/j.poly.2013.10.012openalex-snapshot
Reactions of cyclotriphosphazene with 1,6-diaminohexane and 1,8-diaminooctane: Mono-ansa, double- and triple-bridged derivatives
inferredcites →https://doi.org/10.1016/j.saa.2011.10.027openalex-snapshot
Phosphorus–nitrogen compounds. Part 23: Syntheses, structural investigations, biological activities, and DNA interactions of new N/O spirocyclotriphosphazenes
inferredcites →https://doi.org/10.1016/s0020-1693(00)84319-4openalex-snapshot
An answer to the SPIRO versus ANSA dilemma in cyclophosphazenes. Part VII. Neither SPIRO nor ANSA: the BINOdicyclotriphosphazenes, N3P3Cl5 [HN(CH2)nNH] Cl5P3N3
inferredcites →https://doi.org/10.1016/s0168-3659(03)00199-8openalex-snapshot
Synthesis and antitumor activity of novel thermosensitive platinum(II)–cyclotriphosphazene conjugates
inferredcites →https://doi.org/10.1021/ic00092a013openalex-snapshot
New Mono- and Trispirocyclotriphosphazenes from the Reactions of (NPCl2)3 with Aromatic Ortho Dinucleophiles
inferredcites →https://doi.org/10.1021/ic00234a002openalex-snapshot
Quaternized cyclic and high polymeric phosphazenes and their interactions with tetracyanoquinodimethane
inferredcites →https://doi.org/10.1021/ic049483oopenalex-snapshot
Phosphazene-Based Ionic Liquids: Synthesis, Temperature-Dependent Viscosity, and Effect as Additives in Water Lubrication of Silicon Nitride Ceramics
inferredcites →https://doi.org/10.1021/ic100781vopenalex-snapshot
Phosphorus−Nitrogen Compounds. 21. Syntheses, Structural Investigations, Biological Activities, and DNA Interactions of New N/O Spirocyclic Phosphazene Derivatives. The NMR Behaviors of Chiral Phosphazenes with Stereogenic Centers upon the Addition of Chiral Solvating Agents
inferredcites →https://doi.org/10.1021/ja051042wopenalex-snapshot
Columnar Mesomorphic Organizations in Cyclotriphosphazenes
inferredcites →https://doi.org/10.1021/jo990489iopenalex-snapshot
A Regioselective Route to New Polytopic Receptors by Diaminolysis of Chlorocyclotriphosphazatriene-Containing Crown Ethers
inferredcites →https://doi.org/10.1021/jp004299jopenalex-snapshot
31P and 13C NMR Studies of a Liquid-Crystalline Cyclotriphosphazene Derivative: Orientational Characteristics and Contrasting Shielding Anisotropies for Inorganic and Organic Moieties
inferredcites →https://doi.org/10.1039/b004872kopenalex-snapshot
Phosphazenes as scaffolds for the construction of multi-site coordination ligands
inferredcites →https://doi.org/10.1039/b104973aopenalex-snapshot
Chiral configurations of spermine-bridged cyclotriphosphazatrienes
inferredcites →https://doi.org/10.1039/c5nj01530hopenalex-snapshot
Syntheses, structural characterization and biological activities of spiro-ansa-spiro-cyclotriphosphazenes
inferredcites →https://doi.org/10.1039/dt9760001582openalex-snapshot
A phosphorus-31 nuclear magnetic resonance study of amino-derivatives of the chlorocyclophosphazenes, N3P3Cl6 and N4P4Cl8
inferredcites →https://doi.org/10.1039/dt9800000840openalex-snapshot
Studies of phosphazenes. Part 10. Spirocyclic derivatives of cyclotriphosphazatrienes
inferredcites →https://doi.org/10.1039/j19660000056openalex-snapshot
Phosphorus–nitrogen compounds. Part XIX. The 1 H nuclear magnetic resonance spectra of some geminal ethoxycyclotriphosphazatrienes: virtual coupling with two and three phosphorus atoms
inferredcites →https://doi.org/10.1080/02678292.2013.773093openalex-snapshot
Synthesis of a series of triple-bridged cyclotriphosphazene hexa-alkoxy derivatives and investigation of their structural and mesomorphic properties
inferredcites →https://doi.org/10.1080/03086648708080650openalex-snapshot
SINGLY, DOUBLY AND TRIPLY BRIDGED POLYAZAHETEROPHANES DERIVED FROM HEXACHLOROCYCLOTRIPHOSPHAZENE, N3P3Cl6
inferredcites →https://doi.org/10.1080/10426507.2012.737878openalex-snapshot
Phosphorus-Nitrogen Compounds: The Reactions of Hexachlorocyclotriphosphazatriene with Pentane-1,5-Diol. Nuclear Magnetic Resonance Studies of The Products
inferredcites →https://doi.org/10.1080/10426507.2013.807255openalex-snapshot
Synthesis and Structural Characterization of Singly, Doubly, and Triply Bridged Derivatives of Hexachlorocyclotriphosphazene with Bis(2-hydroxyethyl) Ether and 2,2-dimethylpropane-1,3-diol
inferredcites →https://doi.org/10.1080/10426507.2016.1160238openalex-snapshot
Phosphorus-nitrogen compounds: Reinvestigation of the reactions of hexachlorocyclotriphosphazene with 1,4-butane- and 1,6-hexane-diols—NMR studies of the products
inferredcites →https://doi.org/10.1080/10426508908046081openalex-snapshot
THE REACTIONS OF PHOSPHAZENES WITH DIFUNCTIONAL AND POLYFUNCTIONAL NUCLEOPHILIC REAGENTS
inferredcites →https://doi.org/10.1097/00001813-200010000-00008openalex-snapshot
Synthesis and antitumor activity of cyclotriphosphazene-(diamine)platinum(II) conjugates
inferredcites →https://doi.org/10.1134/s1070363207120079openalex-snapshot
Synthesis, spectral properties, and antimicrobial activity of 2-arilamino-2,4,4,6,6-pentachloro-1,3,5,2λ5,4λ5,6λ5-triazatriphosphines and poly[bis(4-fluorophenylamino)phosphazene]
inferredcites →https://doi.org/10.1139/v72-149openalex-snapshot
Separation of Gas Mixtures by Accommodation Pumping
inferredcites →https://doi.org/10.1146/annurev.pa.35.040195.000415openalex-snapshot
Polyamines as Targets for Therapeutic Intervention
inferredcites →https://doi.org/10.1146/annurev.pharmtox.35.1.55openalex-snapshot
Polyamines as Targets for Therapeutic Intervention
inferredcites →https://doi.org/10.1515/znb-1981-0720openalex-snapshot
Isolation of the Geminal Bis(amido) Derivative, N4P4(NH2)2Cl6, from the Reaction of N4P4Cl8 with Ammonia
inferredcites →https://doi.org/10.1515/znb-1982-1112openalex-snapshot
Derivatives of NPCl2(NSOCl)2 and (NPCl2)2NSOCl, Part XX [1]. Reactions of Some Inorganic Ring Systems with N,N′ -Dimethylethylenediamine
inferredcites →https://doi.org/10.3987/com-88-s17openalex-snapshot
Phosphorus-nitrogen Componds. Part 58. The Reactions of Hexachlorocyclotriphosphazatriene with Ethane-, 1,3-Propane- and 1,4-Butane-Diols. Spiro, Ansa, Bridged and Dangling Derivatives and Their 31P and 1H Nuclear Magnetic Resonance Spectra

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Molecular Design of Transparent Cyclotriphosphazene-Based Elastomers with Tunable Thermal, Mechanical and Flame-Retardant Properties
inferred← citeshttps://doi.org/10.2139/ssrn.4684288openalex-extracted
Molecular Design of Transparent Cyclotriphosphazene-Based Elastomers with Tunable Thermal, Mechanical and Flame-Retardant Properties
inferred← citeshttps://doi.org/10.1002/jccs.202200415openalex-snapshot
Synthesis, structural, and stereogenic characterizations of new trispirocyclotriphosphazenes
inferred← citeshttps://doi.org/10.1007/s11164-025-05603-7openalex-snapshot
Phosphorus-nitrogen compounds. Part 78. Design, synthesis, crystallographic and spectral properties, free radical scavenging and bioactivity studies of tetrakis(alkylamino)monoferrocenyl-(N/N)-spiro-cyclotriphosphazenes
inferred← citeshttps://doi.org/10.1016/j.colsurfa.2026.139620openalex-snapshot
Cyclophosphazene-based polymeric surfactants for emulsion polymerization of fluorinated monomers
inferred← citeshttps://doi.org/10.1016/j.jtice.2024.105898openalex-snapshot
Cyclotriphosphazene-based crosslinked networks with tunable thermal, mechanical, and flame-retardant properties
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.135209openalex-snapshot
Syntheses of tetrachloro and tetraamino(2-furanylmethyl)spiro(N/N) cyclotriphosphazenes: Chemical, structural elucidation, antiproliferative and antimigratory activity studies
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.141926openalex-snapshot
Phosphorus-nitrogen compounds: Part 79. Design and synthesis of spiro-bino-spiro (sbs)-bis (tetraalkylaminocyclotriphosphazenes) and novel twenty-membered bis(dichlorocyclotriphos-phaza)macrocycles: Structural analysis, chirality and bioactivity studies
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.143614openalex-snapshot
Phosphorus-nitrogen compounds: Part 81. Syntheses and characterizations of the novel lithium complexes of monoferrocenylspirocyclotriphosphaza-crown ethers
inferred← citeshttps://doi.org/10.1016/j.porgcoat.2022.106913openalex-snapshot
Interfacial bonding flame retarded coating of nylon 6: Anti-dropping, self-extinguishment and water-proof
inferred← citeshttps://doi.org/10.1021/acsami.0c21968openalex-snapshot
Polyoctahedral Silsesquioxane Hexachlorocyclotriphosphazene Membranes for Hot Gas Separation
inferred← citeshttps://doi.org/10.1039/9781839166198-00355openalex-snapshot
Phosphazenes
inferred← citeshttps://doi.org/10.2139/ssrn.4803946openalex-snapshot
Cyclotriphosphazene-Based Elastomers with Tunable Thermal, Mechanical, and Flame-Retardant Properties
inferred← citeshttps://doi.org/10.35193/bseufbd.1063257openalex-snapshot
Diamino-sübstitüe Halkalı Trifosfazen Türevlerinin Antimikrobiyal Aktivitelerinin Araştırılması
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.